Peritoneal Cancer: Anyone else?
Looking for any help with this thank you
Interested in more discussions like this? Go to the Cancer Support Group.
Looking for any help with this thank you
Interested in more discussions like this? Go to the Cancer Support Group.
Hi Jan, what a story. And what a fish (not a fish story, lol). Like @dntsass01's son's story, your husband's experiences brings hope. I really appreciate your joining this discussion group. I'm sure that @turbo48 @scjoyce and @dorcarvajal will appreciate bouncing things off you and having your support.
Your participation would also be very welcome in the ostomy group here:
- Ostomy https://connect.mayoclinic.org/group/ostomy/
How are you doing with the return of mucin and what lies ahead?
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2 ReactionsHi Dor, I add my welcome. I noticed that you wanted to post a link to an essay you wrote for StatNews with your post. You will be able to add URLs to your posts in a few days. There is a brief period where new members can't post links. We do this to deter spammers and keep the community safe. Clearly the link you wanted to post is not spam. Please allow me to post it for you.
- Male doctors said my ‘female’ cancer was incurable. Then a woman took command and gave me hope https://www.statnews.com/2018/10/04/peritoneal-cancer-women-men-doctors/
It is a beacon of hope to hear you say that you're "savoring my exodus from cancerland." Many cancer survivors, even when there is no evidence of disease (NED), still don't feel like they can truly exit cancerland. There's the regular checkups and scanxiety, and every medical symptom makes one wonder... What is your tip to others to embrace the exit?
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4 ReactionsCongratulations @dorcarvajal!!! You have earned your right to savor your exodus. I truly understand what a milestone this is, as I look forward to the day when I can join you. My 3-year mark will be this fall, I am in remission with NED after a similar treatment experience as yours, although for a different cancer, and my doctors are discussing removing my port. Here's to your continued good health 🙂
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3 ReactionsThanks for posting that essay Coleen. Since I wrote it, I have heard from families all over the world desperate for information about treating this rare form of peritoneal cancer. I wish there was some site that they could turn to for an up to date guide about treatment. Like everyone else, I feel dread every time I have to go for a scan or a blood test for CA125. I simply think in terms of one step forward, fall down, get back up. So far it’s been an incredible relief when the results come in. Meantime, I savor the present.
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6 ReactionsThanks @polkagal. Thrilled for you.
@dorcarvajal What an excellent article! Thank you for writing it, although I’m sorry about the circumstances that got you there. Becky
Thank you. Since I wrote it, I continue to be contacted by families all over the world seeking information about this rare disease. There is a strong need for up to date guides.
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2 ReactionsHave you heard of the book: “Unwell Women: Misdiagnosis and Myth in a Mam-made World” ?
I was dx in Jan 2022 with Primary Peritoneal Cancer. I have battled with repeated UTIs that have caused me to be hospitalized 5 times which delays my Chemo treatments. At the Mayo Clinic now to discuss taking the chemo pill. Anyone else have similar issues?
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1 ReactionHi Pam, please accept my belated welcome. It can be so stressful to have symptoms that cause delays in chemo treatment. I'm sure you just want to stay on track and get rid of this darn cancer.
How did the appointment at Mayo turn out? Is oral chemo a good option for you?